专利摘要:
A composition containing at least one compound of the formula <IMAGE> (I) in which R is alkyl, alkenyl, alkinyl, halogenoalkyl or alkoxyalkyl, R1 is alkoxyalkyl or dialkoxyalkyl, R2 is alkyl or alkoxy, and x is oxygen or sulfur and n is 0, 1, 2 or 3. The compounds have a strong herbicidal effect against various weeds together with a broad selectivity in regard to agricultural plants, particularly potatoes, cotton, peanuts, carrots and rice.
公开号:SU717990A3
申请号:SU782632100
申请日:1978-07-03
公开日:1980-02-25
发明作者:Арндт Фридрих;Борошевски Герхард
申请人:Шеринг Аг (Фирма);
IPC主号:
专利说明:

(54) HERBICID MEANS
  ,; - - -.one . ; ; //
The invention relates to chemical agents for controlling weeds and undesirable vegetation (ai), namely, to a terbicidal agent containing an active principle from among carbohydrate-carboxylic acid derivatives and auxiliary components from a group of liquid or solid nosyogels, surfactants, etc.
A herbicidal agent is known, the active principle of which is E-methoxycarbonylamino-phenyl ester of 3-methylcarbanilic acid and. its analogues 1.
The prototype of the invention is herbicidal agents on the axis of carbamic acid derivatives. These include, for example, an agent based on urethanes-3-Calkyloxy-Idyl-alkylthiocarbonylinol-phenyl esters of M-allyl-N-benelikarbamoyoy acid 2
However, the known herbicidal agents of this group are not sufficiently effective for certain types of weeds and are not selective for crops,
The aim of the invention is a new Herbicidal agent based on carbamic acid derivatives, possessing a pyuyoy gerbicide effect, activity and selectivity of action.
This is achieved by using a carbamic acid derivative of the general formula, 1 -
ten
NHC-XR a)
N-C-O
 alkyl, 2-methoxyethyl,
where R is chloroethyl, bromstil, chloroisopropyl, allyl / propargyl;
R
- alkoxyzistil C, -C, 2,2-dimethoxyethyl, 2,2-diethoxyethyl; ,
-methyl or methoxy; - O or 1;
P
.. - oxygen or sulfur.
X
The content of the active principle in the herbicidal agent ranges from 1 ° C to 80% by weight.
The forms of application of the active substances are ordinary: solutions, emulsions, pastes, powders, etc. They are prepared by known methods.
Recommended doses of the active principle for the selective destruction of weed plants range from 0.5 to 5 kg / ha.
The method of obtaining compounds of the general formula. based on the reaction of the corresponding aryl chloroformates with N-substituted anilines in the presence of a hydrogen chloride accelerator. They are also prepared by reacting 3-acylaminophenols with N-arylcarbamyl chloride or other known methods.
N- (2-methoxyethyl) -car1-carboxylic acid 3- (Мё1 6xycarbonyl mino) -phenyl ester
N- (2,2-dimethoxyethyl) -carbanilic acid 3- (methoxycarbonylamino) -phenyl ester
3- (Methoxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -3-methylcarbanyl acid
3- (Ethoxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -carbanilic acid
3- (Isopropoxy1 arbonylamino) -phenyl ester of N- (2,2-di-methoxyethyl) -carbanilic acid
-. . . ,, ,,,, ..,;,::.,. :: V;, ..., - --- L--
3- (Isopropoxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -carbanilic acid
Z-Sec - Butoxycarbonylamino-phenyl ether of N- (2-methoxyethyl) -carbanyl acid
3-Isobutylcarbonylamino-phenyl ether
N- (2,2-dimethoxyethyl) -carbanyl ACID 3- (2-Methylpropoxycarbonylamino) -phenyl ester of N- (2-methoxyethoxy) -, carbanyl. acids
Z- (Allyloxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -carbanilic acid
Z- (Allyloxycarbonylamino) -phenyl ester of N- (2,2-di1 "5 tethoxyethyl) -carbanyl acid
3- (2-Propynyloxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl) -carbanilic acid
3- (2-Propynyloxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -carbanilic acid - - -
3 (Methylthiocarbonylamino) -phenyl ester of N- (2, 2-dimethoxyethyl) -carbonyl acid
3- (Ethylthiocarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl; -carbanilic acid
1, Post-emergence
Example
experience. .
Experimental plants grown under greenhouse conditions up to a certain stage of development are treated with preparative forms of the active substances with a preparation consumption rate of 600 l / ha, which corresponds to 5 kg / ha of the active substance. Evaluation of the herbicidal action was carried out after 3 weeks post processing. The results of the experiment are given in table. one.
T a
faces
4 4
4 4
Z- (Ethylthiocarbonylamino) -phenyl ester of N- (27-methoxyethyl) -carbanilic acid
3- (Methoxycarbonylamino) -phenyl ester of 1Н- (2-ethoxyethyl) -carbanyl acid
3- (Methoxycarbonylamino) -phenyl ester 1SI- (2-ethoxyethyl) -3-methylcarbanilic acid
3- (Methoxycarbonylamino) -phenyl ester of (2,2-dimethoxyethyl) -3-methylcarbanyl acid
N- (2,2-dimethoxyethyl) -4-methylcarbanyl 3- (methoxycarbonylamino) -phenyl ether
acids
3- (Etoxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -3-methylcarbanyl acid
3- (Ethoxycarbonylamino) -phenyl ester of N- (2-ethoxyethyl) -carbanilic acid
3- (Ethoxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl) -3-methylcarbanilic acid
3- (Ethoxycarbonylamino) -phenyl ester of N- (2-ethoxyethyl) -3-methylcarbayl
acids
3- (Ethoxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl) -4-methylcarbanyl
acids
3- (Isopropoxycarbonylamino) -phenyl ef N- (2,2-dimethoxyethyl) -4-methylcarbanilic acid
N- (2,2-dimethoxyethyl) -3-methylcarbanilic acid 3- (1-methyl-ethoxycarbonylamino) -phenyl ester
Z- (Butoxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl-4-methylcarbanilic acid
N- (2,2-dimethoxyethyl) -3-methylcarbanic acid 3- (2-Methylpro-Opoxycarbonylamino) -phenyl ester
N- (2,2-dimethoxyethyl) -3-methylcarbanilic acid 3- (1-methylpropoxycarbonylamino) -phenyl ester
3- (2-MethylpropoxycarbonylMino) -phenyl ester of N- (2,2-dimethoxyethyl) -4-methylcarboxylic acid
3- (2-Methoxyethoxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl) -3-methylcarbanic acid
Continued tabl, 1
.4 W; .
.7179908 Continued table. 1 SG (Allylxycarbonylamino) -phenyl ether - (2,2-dimethoxyethyl) -3-methylcarbanyl Acid. 4 4 3- (2-Propynyloxycarbonylamino) -phenyl ether N- (2,2-dimethoxyethyl) -3-methylcarb-; nil acid. 44 (3-Methylthiocarbonylamino) -phenyl ester of M- (2-methoxyethyl) -carb; yl-yl acid 4 4 3- (Methitibcarbonylamino) -phenyl ester of N- (2,2-dimethoxistil) -4-methyl-capstanil. acid. . . -. . . . (3-Methylthiocarbonylamino) phenyl ether; N- (2,2-Dimethoxyethyl) -3-methylcarbanyl acid, 44- (3-Ethylthiocarbonylamino) -phenyl ester of N- (2,2- | cymethoxyethyl) -3-methylcarbanyl. . acid. -. . , (3-Ethylthiocarbonylamino) -fevyl ester .H- (2,2-dimethoxyxyethyl) -4-methylcarbanyl. ACIDS, -., ... .V - .... .- ... (3-Methylthiocarbonylamino) -phenyl ester of N- (2-ethoxyethyl) -3-methylcarbanyl / i acid, l. V V :::.; -:;, - ;;,; .,. . ; . . - I (3-Methylthiocarbonylamino) -phenyl ether ... N- (2-methoxyethyl) -4-methylcarbamate acid. Mr..:.-....-,. ;.: ...--.;.: -. . (3-Methylthiocarbonylamino) phenyl ester of L (2-butoxyethyl) 4-methylcarbanilic acid. ...: ...,. :. . . . . (3-Methylthiocarbonlamino) -phenyl ester of y- (2-ethoxyethyl) 1-2-MeGlcarbanil-l4 acid:. (3-Methylthiocarbonylamino) -phenyl Ether. (2-methoxyethyl) -3-methoxycarbanilnry4. V. Acids: ..V. . . ; ....... - N- (2-butoxyethyl) -carbanilic acid (5-methylthiocarbonylamino) -phenyl ester "(3-Ethylthiocarbonylakino) -phenyl ester of Y- (2-methoxyethyl) -4-methoxycarbanilic, acid . H- (2-methoxyethyl) -4-methoxycarbanilic acid 3- (1-Methyloxycarbonylamino) phenyl V ester (3-Methylthiocarbonylamino) phenyl ester of K (2-ethoxy-methyl) carbanilic acid 3- (2-ProPhenyloxycarbonylamino-ayloxy-yl-yl-yl-yl-yl-yl-yloxy) -amoylcarboxylic acid; (2-methoxyethyl) -4-methoxycarbacyl-44 hydrochloric acid ,. 3- (1-methylpropoxycarbonylamino) -phenyl, n- (2-methoxyethyl) -4-methoxy of rbanilyic acid ester
3- (2-Methylpropoxycarbonylamino) phenyl ester of N- (2-methoxyethyl) -4-methoxycarbanilic acid
N- (2-methoxyethyl) -3-methylcarbanilic acid (3-ethylthiocarbonylamino) phenyl ester.
N- (2-methoxyethyl) -3-methylcarbanilic acid 3- (2-methylpropoxycarbonylamino) -phenyl ester
3- (2 / -methylpropoxycarbonylamino) -phenyl ester of N- {2-ethoxyethyl) -carbanilic acid
3- (2-Methylpropoxycarbonylamino) phenyl ester of H- (2-ethoxyethyl) -3-methylcarbanyl 6th acid
3- (1-Methyl Propoxycarbonylamino) Phenyl ester of N- (2-ethoxyethyl) -carbanyl acid
N- (2-methoxyethyl) -carbanyl acid 3- (1-cetyl-2-chloroethoxy-carbonylamino) -phenyl ester.
3- (1-Methyl-2-chloro-hydroxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl) -carbanilic acid
3- (Methylthiocarbonylamino) -phenyl ester N- (2-methoxyethyl) -4-meto, xicarbani; 1 Nt:
N- (2,2-dimethoxyethyl) -carbanyl acid 3- (2-bromoethoxycarbonylamino) -phenyl ester
3- (2-Methoxyethoxyxy (rboylamino) -phenyl ester of N- (2,2-dimethoxyethide) -carbonyl acid
3- (Methylthiocarbonylamino) -phenyl ester of N- (2-methoxyethyl) -2-methylcarbanyl
acids - -..-. l, A „, ..,.-.-. ,, ,, ,, ....
H- (2-Propoxyethyl) -3-methylcarbanyl- 3- (2-Methyl Propoxycarbonylamino) -phenyl ester,
Noah acid.
N- (2-methoxyethyl) -4-methylcarbanilic acid 3- (2-methylpropoxycarbrylamino) -phenyl ester
N- (2-methoxyethyl) -3-methyl-carboxylic acid 3- (1-methylpropoxycarbonylamino) phenyl ester.
(3-Methylthiocarbonylamino) -phenyl ester of 3-methyl N- (2-propoxyethyl) -carbanilic acid /
(3-Allyloxycarbonylamio) -phenyl ester of c- (2-ethoxyethyl) -carbanyl acid
Continued table. I
4 4
-., -. - s
 four
four
four
1171799012
N- {2-ethoxyethyl) -3-methylcarbanyl (3-allyloxycarbonylamino) -phenyl ester
ky eloty.
N- (2-Propoxyethyl) -carbanilic acid (3-allyloxycarbonylamino) -phenyl ester
3- (2-Bromoethoxycarbonylamino) -phenyl, ester of H- (methoxyethyl) -carbanilic acid
3- (Methoxycarbonylamino) -phenyl Ely N- (2-butoxyethyl) -3-methylcarbanilic ester
3- (Ethoxycarbonylamino) -phenyl ester of N- (2-but6xyethyl) -3-methylcarbanilic acid
3- (Etoxycarbonylamino) -phenyl ester of N- (2,2-diethoxyethyl) -carbanilic acid
3- (1-Methylethoxycarbonylamino) -phenyl ester of N- (2-prop6xyethyl) -carbanilic acid -
3- (1-Methylethoxycarbonylamino) -phenyl ester of N- (2-butoxyethyl) -3-methylcarbanilic acid
N- (2-Propoxyethyl) -3-methylcarbanilic acid 3- (1-Methyltoxycarbonylamino) phenyl ester,
3- (1-Methylethoxycarbonylamino) -phenyl ester of N- (2-butoxyethyl) -4-methylcarbanyl acid
3- (1-Methylethoxycarbonylamino) -phenyl ester of N- (2-butoxyethyl) -carbanyl acid
N- (2,2-Diethoxyethyl) -carbanyl acid (3-allyloxycarbonylamino) -phenyl ester
3- (2-Propenyloxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -2-methylcarbanyl acid
3- (2-Methylpropoxycarbonylamino) phenyl ester of N- (2,2-daethoxyethyl) -carbanilic acid,
N- (2,2-diethoxyethyl) -carbanyl 3- (2-Propynyloxycarbonylamino) -phenyl ester
acid. ;
Z- (Methylthiocarbonylamino) -phenyl ester of N- (2-ethoxyethyl) -4-methylcarbanilic acid
3- (Methylthiocarbonylamino) -phenyl ester of N- (2,2-diethoxyethyl) -carbanilic acid
{s-Methylthiocarbonylamino-phenyl ester of N- (2-propoxyethyl) -4-methylcarbanyl
acids
Continued table. one
(3-Methylthiocarbonylamino) phenyl ester of - (2-propoxyethyl) -2-methylcarbanilic acid
(3-Methylthiocarbonylamino) phenyl ester of - (2-butoxyethyl) -3-methylcarbanilic acid
(3-EthylthiocarbonylsMine6) -phenyl ether. N- (2-propoxyethyl) -3 methylcarbanilic acid. . i.
(3-ethylthiocarbonylamino) -phenyl ether - (2-butoxyethyl) -3-methylcarbanilic acid
(3-Ethylthiocarbonylamino) -phenyl ether - (2-butoxyethyl) -4-methylcarbanyl
acids
N- (2-cyanoethyl) -3-chlorocarbayl acid ((Z-allyloxycarbonylamino) -phenyl ester
3- (2-Propyloxycarbonylamino) -phenyl ester of N- (2-propyloxyethyl) -3-methylcarbanilic acid
3- (2-Propynyloxycarbonylamino) -phenyl ester of N- (2-propoxy ethyl) -carbanilic acid
3- (2-Propynyloxycarbonylamine) phenyl ester of H- (2-butoxyet.til) -4-methylcarbanilic acid. N- (2-butoxyethyl) -carbanyl acid 3- (2-PropinyloxycarbonylIlamino) -phenyl ester
3- (2-propynyloxycarbonylamino) -phenyl ester of H- (2-propoxy-yl) -2-methylcarbanilic acid
N- (2-Butoxyethyl) -3-methylcarbanilic acid 3- (2-propynyloxycarbonylamino) phenyl ester;
N- (2-Propoxyethyl) -4-methylcarbanilic acid 3- (2-propynyloxycarbonylamino) phenyl ester.
(3-Ethylthiocarbonylamino) -phenyl ester of - (2-ethoxyethyl) -carbanyl acid
(.3-Ethylthiocarbonylamino) -phenyl ester of - (2-ethoxyethyl) -3-methylcarbanilic acid
(3-Ethylthiocarbonylamino) -phenyl; o-ester of - (2-propoxyethyl) -2-methylcarbanyl acid
(3-Ethylthiocarbonylamino) phenyl ester of N (2-ethoxyethyl) -4-methylcarbanilic acid
Continued table. one
权利要求:
Claims (2)
[1]
 V - ipf r #., ": 7 gpk p oprnki- o - no action G4 humiliation SacTe ml ep
[2]
2. Experimental plants. PREMIRE 2. Experimental plants 6br2b2yyyyytyy ypiy after exits,. ..., .. ,, -.--: -.----. ,,,., .- .. yormGraskhoDa 1 kg of aytyvnogo-. Begin / ha For comparison, take | 3-mv xycadH nile-3-phenyl 1571799016 ---- G- 1- 1 3 4 -: ..--, -. -J .., -.-: -:., ..-- -.;. , v., -. ,;, -.... -T -.,.; .-. I..i .- .. ji, r ..-. - ,,. .-- L-. ---. - .--.-- ... (3-Ethylthiocarbonylamino) -phenyl ester of M- (2-propoxyethyl) -4-methylcarbanilic acid -: - (3-Ethylthiocarbonylamino) -phenyl ester of N- (2-meToxyethyl) -4 -methylcarb; nyl acid V, (3-Ethylthiocarbonylamino) -phenyl ester of N- (2-ethoxyethyl) -2-methylcarbanilic acid 1. (3-Ethylthiocarbonylamino) -phenyl ester of 1Н- (2-methoxyethyl) -3-methoxycarbanyl acid, -. - (3-Methylthio arbonylamino) -phenyl ester of N- (2-methoxyethyl) -3-methylcarbanilic acid. "...., -, -SZ" L "J (3-Ethoxycarbonylamino) -phenyl ester of 2-methyl L- (2-Propoxyethyl) -carbanilic acid 3- (1-Methylethoxycarbonylamino) phenyl ester of H- (2-ethoxyethyl) carbanyl acid 3- (1-Methyl ethoxycarbonylamino) phenyl ester of H- (2-methoxyethyl) t-4-methyloxyphenyl ester of 3- (2-methoxyethyl) t-4-methyle-phenyl ester of O- (2-methoxyethyl) t-4-methyle) -phenyl ester of O- (2-methoxyethyl) t-4-methyle) -phenyl ester of N- (2-methoxyethyl) t-4-methyyl-phenyl ester of (- (2-methoxyethyl) t-4-methyyl-phenyl ester of - (2-methoxyethyl) t-4-methyyl-phenyl ester of Ы- (2-methoxyethyl) t-4-methyl; acids: N- {2-1-1 -Cisistil) -4-methylcarbanilic acid 3- (1-methyl-ethoxycarbonylamino) -phenyl ester -f3- (1-methyl-ethoxycarbynylamino) -phenyl-1-methyl-1-methyl-1-methyl 1-methyl-1-ester th acid - L. -1--, x- - 3- (1-Methyloethoxycarbonyl-amino-phenyloyl 4-methyl N- (2-prrpoysi9Tyl) ester) -carbanyl acid V i 3 (Ethoxy-arbonylamino) -phenyl 4-methyl-L- ester (2-propO | C IETHYL) -carbanilic acid. 3- (1-Methyl ethoxycarbonylgarynol) -phenyl ester IN- (2-ethoxyethyl-3-methyLcarbanillic acid; 3- {1-Methyl ethoxycarbonylamino) -phenyl ester S- ( 2-ethoxyethyl) -2-methylcarbanilic acid Continued table. 1 3-methylcarbanilic ester (Compound A). The plants were 60 In the early stage of development. Liquids take 500 l / ha. Means nands t .., .. g - "-.-, l" in the form of a water emulsion, after 14 days - .. .. .. 1. "" Tk. I l evaluate the results of processing. Rating scale: 10 - no damage; About - the destruction of plants. 17 In table. 2 shows comparative data on the herbicidal activity of the proposed and known compounds. It has been shown that when compatible with cultivated plants of the ped. Table 2 of these compounds achieve a good effect on the weeds, while the comparative remedy severely damages cultivated plants. 19 Claims Herbicidal agent containing a derivative of carbamic acid as an active principle, as well as auxiliary components, selected from a group of liquid or solid carriers of surfactants, with the aim of increasing herbicidal activity and improve the selectivity of action, as a carbamic acid derivative, a compound of the general formula
€ # 4 B5 - 0 de R - alkyl C; - Qj, 2-methoxyethyl, hlrethyle, bromoethyl, chloro; Isopropyl, ally, propargyl; R - alkoxyethyl, 2,2-dimethoxyethyl, 2,2-diethoxyethium; R is MeTHJi or Metxy; p - O or I) to acid 6) rb or, in an amount from GO to 80 wt.%. Sources of information taken into account in the examination 1.Patent of the Federal Republic of Germany 1567151 cl. 12 about 17/01, publ. 21.b2.74, 2.Patent of Germany W2310648, kL. 12 from 17/01, 19.09.74 (prototype).
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同族专利:
公开号 | 公开日
IT7825741D0|1978-07-17|
CA1103268A|1981-06-16|
AU519399B2|1981-12-03|
PL111138B1|1980-08-30|
IT1097530B|1985-08-31|
CS197327B2|1980-04-30|
FR2398053B1|1982-11-19|
BE869074A|1979-01-18|
GB2002356B|1982-03-03|
JPS5422340A|1979-02-20|
FR2398053A1|1979-02-16|
DD137822A5|1979-09-26|
CH637372A5|1983-07-29|
GR73026B|1984-01-25|
IL55156A|1982-11-30|
IE47234B1|1984-01-25|
DK320778A|1979-01-19|
PL208435A1|1979-03-26|
GB2002356A|1979-02-21|
PT68309A|1978-08-01|
ES471736A1|1979-02-01|
US4441915A|1984-04-10|
NL7807482A|1979-01-22|
IE781440L|1979-01-18|
HU180531B|1983-03-28|
SU858561A3|1981-08-23|
LU79980A1|1978-12-12|
AU3810478A|1980-01-24|
IL55156D0|1978-09-29|
DE2732848A1|1979-02-08|
引用文献:
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法律状态:
优先权:
申请号 | 申请日 | 专利标题
DE19772732848|DE2732848A1|1977-07-18|1977-07-18|DIURETHANE, HERBICIDAL AGENTS CONTAINING THESE COMPOUNDS AND THE PROCESS FOR THEIR PRODUCTION|
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